FDA 510(k)

第三只眼全景辅助内窥镜系统 - 负责人

K号: K160356 · 2016-05-17

决定日期2016-05-17

产品代码FDF

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决定实质等同

器械摘要

Third Eye Panoramic Auxiliary Endoscopy System - Resposable is the device name listed in this FDA 510(k) record. The listed applicant is Avantis Medical Systems, Inc.. It received FDA 510(k) clearance on 2016-05-17 under 510(k) number K160356. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Third Eye Panoramic Auxiliary Endoscopy System - Resposable?

Third Eye Panoramic Auxiliary Endoscopy System - Resposable is a medical device that received FDA 510(k) clearance on 2016-05-17. The listed applicant is Avantis Medical Systems, Inc.. The 510(k) number is K160356.

When did Third Eye Panoramic Auxiliary Endoscopy System - Resposable receive FDA 510(k) clearance?

Third Eye Panoramic Auxiliary Endoscopy System - Resposable received FDA 510(k) clearance on 2016-05-17, under 510(k) number K160356.

Who is the listed applicant for Third Eye Panoramic Auxiliary Endoscopy System - Resposable?

The FDA 510(k) record lists Avantis Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Third Eye Panoramic Auxiliary Endoscopy System - Resposable?

The FDA product code for Third Eye Panoramic Auxiliary Endoscopy System - Resposable is FDF.

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第三只眼全景辅助内窥镜系统 - 负责人

器械摘要

常见问题

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